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FDA 510(k)

1-M GRADUATED COMPRESSION ANTI-EMBOLISM STOCKING, MODEL SS-811, SS-508, SS-613

K-Number: K092892 · 2010-08-03

Decision Date2010-08-03
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

1-M GRADUATED COMPRESSION ANTI-EMBOLISM STOCKING, MODEL SS-811, SS-508, SS-613 is the device name listed in this FDA 510(k) record. The listed applicant is I-Ming Sanitary Materials Co., Ltd.. It received FDA 510(k) clearance on 2010-08-03 under 510(k) number K092892. The device is classified under product code DWL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1-M GRADUATED COMPRESSION ANTI-EMBOLISM STOCKING, MODEL SS-811, SS-508, SS-613?

1-M GRADUATED COMPRESSION ANTI-EMBOLISM STOCKING, MODEL SS-811, SS-508, SS-613 is a medical device that received FDA 510(k) clearance on 2010-08-03. The listed applicant is I-Ming Sanitary Materials Co., Ltd.. The 510(k) number is K092892.

When did 1-M GRADUATED COMPRESSION ANTI-EMBOLISM STOCKING, MODEL SS-811, SS-508, SS-613 receive FDA 510(k) clearance?

1-M GRADUATED COMPRESSION ANTI-EMBOLISM STOCKING, MODEL SS-811, SS-508, SS-613 received FDA 510(k) clearance on 2010-08-03, under 510(k) number K092892.

Who is the listed applicant for 1-M GRADUATED COMPRESSION ANTI-EMBOLISM STOCKING, MODEL SS-811, SS-508, SS-613?

The FDA 510(k) record lists I-Ming Sanitary Materials Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 1-M GRADUATED COMPRESSION ANTI-EMBOLISM STOCKING, MODEL SS-811, SS-508, SS-613?

The FDA product code for 1-M GRADUATED COMPRESSION ANTI-EMBOLISM STOCKING, MODEL SS-811, SS-508, SS-613 is DWL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: DWL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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